WO2009069985A1 - Porous light weight iron and method for preparing the same - Google Patents
Porous light weight iron and method for preparing the same Download PDFInfo
- Publication number
- WO2009069985A1 WO2009069985A1 PCT/KR2008/007083 KR2008007083W WO2009069985A1 WO 2009069985 A1 WO2009069985 A1 WO 2009069985A1 KR 2008007083 W KR2008007083 W KR 2008007083W WO 2009069985 A1 WO2009069985 A1 WO 2009069985A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- iron
- porous lightweight
- weight
- lightweight iron
- preparing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/10—Sintering only
- B22F3/11—Making porous workpieces or articles
- B22F3/1146—After-treatment maintaining the porosity
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B13/00—Making spongy iron or liquid steel, by direct processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F5/00—Manufacture of workpieces or articles from metallic powder characterised by the special shape of the product
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F7/00—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression
- B22F7/002—Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of porous nature
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B5/00—General methods of reducing to metals
- C22B5/02—Dry methods smelting of sulfides or formation of mattes
- C22B5/06—Dry methods smelting of sulfides or formation of mattes by carbides or the like
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/08—Alloys with open or closed pores
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C26/00—Alloys containing diamond or cubic or wurtzitic boron nitride, fullerenes or carbon nanotubes
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C32/00—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ
- C22C32/0047—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents
- C22C32/0052—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only carbides
- C22C32/0063—Non-ferrous alloys containing at least 5% by weight but less than 50% by weight of oxides, carbides, borides, nitrides, silicides or other metal compounds, e.g. oxynitrides, sulfides, whether added as such or formed in situ with carbides, nitrides, borides or silicides as the main non-metallic constituents only carbides based on SiC
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/02—Making ferrous alloys by powder metallurgy
- C22C33/0235—Starting from compounds, e.g. oxides
Definitions
- the present invention relates to porous lightweight iron and a method for preparing the same, and more particularly to porous lightweight iron having decreased weight due to pores formed therein while having a strength similar to that of existing steel products; and a method for preparing porous lightweight iron having desired properties or various properties according to intended use.
- porous materials which refer to materials with a pore volume of 10 to 98% based on the total volume, have properties such as impact energy absorption capability, gas and liquid permeability, sound shield, low thermal conductivity, electrical insulation and the like due to pores therein and thus, have been widely used as impact absorbing materials, filters, sound shielding materials, insulators and are also expected to be commercially utilized in more fields. Also, the porous materials are expected to be applied as a lightweight structure, a core material of sandwich structure and the like.
- porous metal and alloy materials known in the prior art include aluminum (Al), magnesium (Mg), zinc (Zn), iron (Fe), lead (Pb), gold (Au), silver (Ag), zirconium (Zr), copper (Cu), nickel (Ni), titanium (Ti), cobalt (Co), nickel-chromium (Ni-Cr) alloy and stainless steel and the like.
- porous metal and alloy materials are used in various fields.
- materials used as impact absorbing materials and structural materials include aluminum (Al), copper (Cu), Nickel (Ni) and the like
- examples of materials used as filtering materials include copper (Cu), stainless steel, gold (Au) and Nickel (Ni)
- materials used as sound shielding materials include copper (Cu).
- a metal porous body As an example of pore-containing metal, a metal porous body (WO 2003/070401) was recently disclosed.
- the metal porous body is prepared by fusing a metal alloy comprising iron, nickel, copper and the like and dissolving a gas into the fused metal material, followed by cooling. It is a lightweight iron material and has a tensile strength comparable to non-porous iron materials, as well as a high strength. Therefore, it is expected to substitute for iron.
- the preparation process and the setting of conditions for the preparation process are complicated, and thus, industrialization thereof is not easy.
- the present inventors have made extensive efforts to develop a substitute for the existing heavyweight stainless steels, and studies and, as a result, confirmed that, when lightweight iron is prepared using metallic minerals, or a mixture of metallic materials and non-metallic materials, the weight of the lightweight iron can be decreased by adding diamond or silicon carbide to form pores inside the iron body, and a lightweight iron having desired properties and effects can be prepared by controlling sintering temperature and addition ratio of diamond or silicon carbide in the preparation process, thereby completing the present invention.
- the present invention provides a method for preparing a porous lightweight iron, which comprises the steps of (a) pulverizing a metallic mineral; (b) mixing 100 parts by weight of the pulverized product obtained in the step (a) with 2 to 20 parts by weight of diamond or silicon carbide; (c) sintering the mixture obtained in the step (b) in a sintering furnace at a temperature of 1100 to 1400 ° C for 2 to 5 hours; and (d) obtaining the resulting porous lightweight iron after completion of the sintering.
- the present invention also provides a method for preparing a porous lightweight iron, which comprises the steps of (a) mixing 100 parts by weight of molten pig iron from a blast furnace with 2 to 10 parts by weight of silicon carbide; (b) sintering the mixture obtained in the step (a) in a sintering furnace at a temperature of 1100 to 1400 ° C for 2 to 5 hours; and (c) obtaining the resulting porous lightweight iron, after completion of the sintering.
- the present invention also provides a porous lightweight iron, which is prepared by the method and has a weight per unit volume of 10 to 65 % (w/v) compared to the existing stainless steel.
- FIG. 1 is a flow chart showing a process for preparing the porous lightweight iron according to the present invention.
- FIG. 2 is a photograph of the porous lightweight iron having various shapes, prepared by the method according to the present invention, using metallic minerals and diamond or silicon carbide.
- FIG. 3 is a photograph of the porous lightweight iron, prepared by the method according to the present invention, using molten pig iron and silicon carbide.
- the present invention relates to a method for preparing a porous lightweight iron, which comprises the steps of (a) pulverizing a metallic mineral; (b) mixing 100 parts by weight of the pulverized product of the step (a) with 2 to 20 weight parts of diamond or silicon carbide; (c) sintering the mixture from the step (b) in a furnace at a temperature of 1100 to 1400 °C for 2 to 5 hours; and (d) obtaining the resulting porous lightweight iron after completing the sintering (FIG.
- a non-metallic mineral may preferably be added and pulverized together with the metallic mineral in the step (a), wherein the non- metallic mineral is preferably added in an amount of 2 to 150 weight parts, based on 100 parts by weight of the metallic minerals.
- the metallic mineral includes at least one selected from the group consisting of iron ore, scheelite, ilmenite, rhodochrosite, lead ore, zinc ore, stainless steel, nickel, chromium, cast iron, scrap iron, Molybdenum ore, tungsten, zirconium ore and iron sulfide.
- the non-metallic mineral includes at least one selected from the group consisting of zeolite, bentonite, limestone, silica sand, dolomite, bauxite, silica stone and fluorite.
- the non-metallic mineral has a low thermal conductivity, and thus, can endure high temperature for a long period of time. Therefore, when the lightweight iron prepared using such non-metallic minerals is applied to building structures, it is expected to show excellent fire resistance.
- the metallic minerals and the non-metallic mineral can be selected from the above mentioned minerals according to the intended use of the final lightweight iron.
- the lightweight iron according to the present invention should be prepared to have decreased weight as well as a strength strong enough to substitute for the existing steel products. Therefore, it can be prepared using minerals, particularly, metallic minerals alone or in combination with non-metallic minerals.
- diamond or silicon carbide is preferably used as an additive to form pores in the porous lightweight iron. They are non-toxic minerals, melt only at a high temperature, and form pores during the sintering process, thus resulting in the effect of producing the resulting lightweight iron.
- the amount of diamond or silicon carbide used in the preparation of the lightweight iron is preferably 2 to 20 parts by weight, based on 100 parts by weight of the metallic mineral or 100 parts by weight of the mixture of the metallic mineral and the non-metallic mineral.
- the method for preparing the porous lightweight iron according to the present invention includes a sintering process, in which if the sintering temperature is less than 1100 ° C , the sintering time is lengthened. If the temperature exceeds 1400 °C , although the sintering time is shortened, the pore size becomes so big that the strength of the resulting lightweight iron is deteriorated. Also, when the sintering time is less than 2 hours, the size of the pores formed inside the iron is small, and when the sintering time exceeds 5 hours, the number of the pores is reduced, whereby the effect of lightweight iron cannot be achieved. Therefore, in the present invention, the sintering temperature and the sintering time of the sintering process is preferably 1100 to 1400 °C and 2 to 5 hours, respectively.
- the volume of the lightweight iron is increased.
- the increased volume of the resulting lightweight iron is 1.5 to 9 times the original volume.
- the prepared lightweight iron cannot be used for the desired purpose. Therefore, in order to prevent such an excessive volume increase, volume of the lightweight iron during the sintering process can be controlled. That is, in order to reduce the extent of volume increase during the sintering process, the sintering temperature is set to the maximum temperature, at which the lightweight iron is not deformed and maintains its original properties, then the sintering process is performed for 20 minutes to 1 hour at that temperature.
- the present invention relates to a porous lightweight iron prepared by the method described above (FIG. 2).
- the porous lightweight iron preferably has a pore size of 0.1 to 1 cm.
- the pore size is closely related with the temperature of the sintering process. That is, if the temperature in a furnace is slowly increased, the pore size is small and the size distribution is uniform, while if the temperature is rapidly increased, the pore size is big and the size distribution is not uniform.
- the porous lightweight iron has a weight per unit volume of 10 to 65 kg (w/v), whereas the general steel has a weight per unit volume of 100 kg, and thus, it is suggested that the porous lightweight iron according to the present invention has a weight of 10 to 65% weight, compared to the existing steel having the same volume. Furthermore, the porous lightweight iron according to the present invention can have 10 to 90% weight, compared to the steel having the same volume, according to the mixing ratio of raw materials used for its preparation.
- the porous lightweight iron has a high packing density, and has excellent compressive strength since it is completely sintered through the sintering process at the high temperature. Also, it has excellent fire resistance since the pores are formed in the sintering process at the high temperature, and has a weight of about 1/20 of the weight of sand having the same volume due to the porosity. Further, the porous lightweight iron can act as an excellent latent heat storage due to the pores formed therein and thus can prevent heat loss, and it shows excellent heat insulation delays heat transmission when a fire occurred to provide escape time, thus making it possible to have the effect of reducing loss of life. In addition, since the porous lightweight iron has decreased weight, it is possible to reduce production costs when applied to an actual industry.
- the present invention relates to a method for preparing a porous lightweight iron, which comprises the steps of: (a) mixing 100 parts by weight of molten pig iron a blast furnace with 2 to 10 parts by weight of silicon carbide; (b) sintering the mixture obtained in the step (a) in a sintering furnace at a temperature of 1100 to 1400°C for 2 to 5 hours; and (c) obtaining the resulting porous lightweight iron, after the completion of the sintering.
- the molten pig iron from the blast furnace has a temperature of 1000 to 2000 °C .
- the temperature of the molten pig iron is less than 1000°C , the reaction with silicon carbide is not sufficient.
- it exceeds 2000 0 C there is no benefit according to the increase in the processing temperature.
- the step (a) is preferably performed for 1 to 8 minutes.
- the reaction time is less than 1 minute, the molten pig iron fails to sufficiently react with silicon carbide, and when it exceeds 8 minutes, there is no benefit according to at the cost of the increase in the processing time.
- the sintering temperature and the sintering time is preferably 1100 to 1400 °C and 2 to 5 hours, respectively.
- Example 1 Preparation of porous lightweight iron using iron ore, zeolite and diamond
- the porous lightweight iron was prepared using iron ore as a metallic mineral, zeolite as a non-metallic mineral and diamond. 96 kg of iron ore and 2 kg of zeolite were pulverized to a particle size of 50 to 120 mesh and mixed with 2 kg of diamond by using a blender. The mineral mixture was sintered at a temperature of 1200 ° C for 5 hours in a sintering furnace to obtain the porous lightweight iron.
- the porous lightweight iron was prepared using iron ore as a metallic mineral, bentonite as a non-metallic mineral and diamond. 90 kg of iron ore and 5 kg of bentonite were pulverized to a particle size of 50 to 120 mesh and mixed with 5 kg of diamond by using a blender. The mineral mixture was sintered at a temperature of 1180 ° C for 5 hours in a sintering furnace to obtain the porous lightweight iron.
- Example 3 Preparation of porous lightweight iron using iron ore, zeolite and diamond
- the porous lightweight iron was prepared using iron ore as a metallic mineral, zeolite as a non-metallic mineral and diamond. 80 kg of iron ore and 10 kg of zeolite were pulverized to a particle size of 50 to 120 mesh and mixed with 10 kg of diamond by using a blender. The mineral mixture was sintered at a temperature of 1250 "C for 4 hours in a sintering furnace to obtain the porous lightweight iron.
- Example 4 Preparation of porous lightweight iron using iron ore, zeolite, limestone and diamond
- the porous lightweight iron was prepared using iron ore as a metallic mineral, zeolite and limestone as non-metallic minerals, and diamond. 70 kg of iron ore, 20 kg of zeolite and 5 kg of limestone were pulverized to a particle size of 50 to 120 mesh and mixed with 5 kg of diamond by using a blender. The mineral mixture was sintered at a temperature of 1150°C for 3 hours in a sintering furnace to obtain the porous lightweight iron.
- the porous lightweight iron was prepared using iron ore as a metallic mineral and diamond. 90 kg of iron ore was pulverized to a particle size of 50 to 120 mesh and mixed with 10 kg of diamond by using a blender. The mineral mixture was sintered at a temperature of 1350°C for 3 hours in a sintering furnace to obtain the porous lightweight iron.
- Example 6 Preparation of porous lightweight iron using iron ore, zeolite, SiO 2 , limestone and diamond
- the porous lightweight iron was prepared using iron ore as a metallic mineral, zeolite, SiO 2 and limestone as non-metallic minerals, and diamond. 65 kg of iron ore, 22 kg of zeolite, 4 kg of SiO 2 and 4 kg of limestone were pulverized to a particle size of 80 to 120 mesh and mixed with 5 kg of diamond by using a blender. The mineral mixture was sintered at a temperature of 1100 ° C for 3 hours in a sintering furnace to obtain the porous lightweight iron.
- Example 7 Preparation of porous lightweight iron using scrap iron, zeolite and diamond
- the porous lightweight iron was prepared using scrap iron as a metallic mineral, zeolite as a non-metallic mineral and diamond.
- 96 kg of scrap iron and 2 kg of zeolite were pulverized to a particle size of 50 to 120 mesh and mixed with 2 kg of diamond by using a blender.
- the mineral mixture was sintered at a temperature of 1200 °C for 4 hours in a sintering furnace to obtain the porous lightweight iron.
- Example 1 to Example 7 The weight of each porous lightweight iron prepared in Example 1 to Example 7 was compared with that of the existing iron steel which was prepared using 100% iron. Each the porous lightweight and the iron steel was measured for their weight per unit volume using a weight measurement device.
- the iron steel had 100 kg of a weight per unit volume and each porous lightweight iron prepared in Examples 1-7 had 38 to 56 kg of a weight per unit volume, as shown in Table 1, which was 38 to 56 % of the weight per unit volume of the iron steel. Therefore, it was confirmed that the porous lightweight irons according to the present invention was lighter than the existing iron steel.
- Example 8 Preparation of porous lightweight iron using molten pig iron and silicon carbide
- the porous lightweight iron was prepared using molten pig iron from a blast furnace and silicon carbide. 100 kg of the molten pig iron heated at a temperature of 1500 ° C in the furnace was mixed with 6 kg of silicon carbide powder for 5 minutes. The mixture was sintered at a temperature of 1250 °C for 4 hours in a sintering furnace to obtain the porous lightweight iron.
- the weight of porous lightweight iron prepared in Example 8 was compared with that of the iron steel which was prepared using 100% iron. Each the porous lightweight iron and the iron steel was measured for their weight per unit volume using a weight measurement device.
- the iron steel had 100 kg of weight per unit volume and the porous lightweight iron prepared in Example 8 had 40 to 60 kg of weight per unit volume, which was 40 to 60% of weight per unit volume of the iron steel. Therefore, it was confirmed that the porous lightweight iron prepared in Example 8 was lighter than the existing iron steel (FIG. 3).
- the thickness, weight and strength of lightweight iron to be produced can be controlled, thus making it possible to prepare porous lightweight iron having desired properties by controlling the sintering temperature during the preparation process, the mixing ratio of diamond or silicon carbide and the mixing ratio of raw materials. Also, since the porous lightweight iron prepared according to the present invention has a weight per unit volume of 10 to 65% (W/V), compared to the existing iron steel products, it is possible to increase economic efficiency and improve processing convenience, when applied to an actual industry.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Composite Materials (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Powder Metallurgy (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Abstract
Description
Claims
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/745,121 US8414827B2 (en) | 2007-11-30 | 2008-12-01 | Porous light weight iron and method for preparing the same |
| JP2010535889A JP2011505495A (en) | 2007-11-30 | 2008-12-01 | Porous lightweight iron and method for producing the same |
| ZA2010/06490A ZA201006490B (en) | 2007-11-30 | 2010-05-28 | Porous light weight iron and method for preparing the same |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR10-2007-0124008 | 2007-11-30 | ||
| KR1020070124008A KR100985231B1 (en) | 2007-11-30 | 2007-11-30 | Porous lightweight body and its manufacturing method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2009069985A1 true WO2009069985A1 (en) | 2009-06-04 |
Family
ID=40678779
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/KR2008/007083 Ceased WO2009069985A1 (en) | 2007-11-30 | 2008-12-01 | Porous light weight iron and method for preparing the same |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8414827B2 (en) |
| JP (1) | JP2011505495A (en) |
| KR (1) | KR100985231B1 (en) |
| WO (1) | WO2009069985A1 (en) |
| ZA (1) | ZA201006490B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100973744B1 (en) * | 2007-12-20 | 2010-08-04 | 이세린 | Porous plant-containing medium containing inorganic materials and method for producing same |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55154534A (en) * | 1979-04-12 | 1980-12-02 | Kobe Steel Ltd | Iron ore porous pellet and its manufacture |
| KR20000000464A (en) * | 1999-10-26 | 2000-01-15 | 이세린 | a method of preparation for ultra light-weight, porous, inorganic material and a material thereof |
| US20020170391A1 (en) * | 2001-05-19 | 2002-11-21 | Wilfried Knott | Production of metal foams |
| KR20070047526A (en) * | 2005-11-02 | 2007-05-07 | 주식회사 엘지화학 | Ultralight ceramic panel and manufacturing method thereof |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2467528A (en) * | 1949-04-19 | Manufacture of shaped metal | ||
| US2110066A (en) * | 1935-05-09 | 1938-03-01 | Heuer Russell Pearce | Iron and steel desulphurization |
| DD109663A5 (en) * | 1973-02-23 | 1974-11-12 | ||
| US4350523A (en) * | 1979-04-12 | 1982-09-21 | Kabushiki Kaisha Kobe Seiko Sho | Porous iron ore pellets |
| SE457537B (en) * | 1981-09-04 | 1989-01-09 | Sumitomo Electric Industries | DIAMOND PRESSURE BODY FOR A TOOL AND WAY TO MANUFACTURE IT |
| US4472351A (en) * | 1983-05-05 | 1984-09-18 | Uop Inc. | Densification of metal-ceramic composites |
| JPS60177992A (en) * | 1984-02-24 | 1985-09-11 | Mazda Motor Corp | Method for joining porous member and its product |
| DE3583567D1 (en) * | 1984-09-08 | 1991-08-29 | Sumitomo Electric Industries | SINTERED DIAMOND TOOL BODY AND METHOD FOR PRODUCING IT. |
| JP3183804B2 (en) * | 1995-03-30 | 2001-07-09 | 株式会社豊田中央研究所 | Porous reinforced sintered body and method for producing the same, composite material using this porous reinforced sintered body and method for producing the same |
| ATE509718T1 (en) * | 2002-02-22 | 2011-06-15 | Hideo Nakajima | METHOD FOR PRODUCING POROUS METAL BODY |
-
2007
- 2007-11-30 KR KR1020070124008A patent/KR100985231B1/en not_active Expired - Fee Related
-
2008
- 2008-12-01 US US12/745,121 patent/US8414827B2/en not_active Expired - Fee Related
- 2008-12-01 WO PCT/KR2008/007083 patent/WO2009069985A1/en not_active Ceased
- 2008-12-01 JP JP2010535889A patent/JP2011505495A/en active Pending
-
2010
- 2010-05-28 ZA ZA2010/06490A patent/ZA201006490B/en unknown
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55154534A (en) * | 1979-04-12 | 1980-12-02 | Kobe Steel Ltd | Iron ore porous pellet and its manufacture |
| KR20000000464A (en) * | 1999-10-26 | 2000-01-15 | 이세린 | a method of preparation for ultra light-weight, porous, inorganic material and a material thereof |
| US20020170391A1 (en) * | 2001-05-19 | 2002-11-21 | Wilfried Knott | Production of metal foams |
| KR20070047526A (en) * | 2005-11-02 | 2007-05-07 | 주식회사 엘지화학 | Ultralight ceramic panel and manufacturing method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| KR100985231B1 (en) | 2010-10-05 |
| US20100303663A1 (en) | 2010-12-02 |
| ZA201006490B (en) | 2011-05-25 |
| JP2011505495A (en) | 2011-02-24 |
| KR20090056728A (en) | 2009-06-03 |
| US8414827B2 (en) | 2013-04-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US11407028B2 (en) | Syntactic metal matrix materials and methods | |
| Mondal et al. | Microwave sintering of refractory metals/alloys: W, Mo, Re, W-Cu, W-Ni-Cu and W-Ni-Fe alloys | |
| CN110423930A (en) | A kind of high entropy ceramic-metal composite of Ultra-fine Grained and preparation method thereof | |
| CN103771892B (en) | Metal strengthening ceramic wafer and preparation method thereof | |
| CN109261980A (en) | A kind of preparation method of heavy alloy tungsten powder | |
| CN102560215A (en) | A Ni3Al-bonded ultra-fine-grained tungsten carbide-based hard alloy and its preparation method | |
| Kumar et al. | A study on thermal behavior of aluminum cenosphere powder metallurgy composites sintered in microwave | |
| Veerappan et al. | Characterization and properties of silicon carbide reinforced Ni-10Co-5Cr (Superalloy) matrix composite produced via powder metallurgy route | |
| CN105018815A (en) | High-Cr-content high-pressure-resistance copper-chromium contact material and manufacturing method thereof | |
| CN109837415A (en) | A kind of manufacturing method of foam aluminium alloy | |
| Cai et al. | Porous NbAl3/TiAl3 intermetallic composites with controllable porosity and pore morphology prepared by two-step thermal explosion | |
| Xie et al. | Effect of ball milling time on the microstructure and compressive properties of the Fe-Mn-Al porous steel | |
| CN103469119B (en) | Amorphous composite materials, and preparation method and applications thereof | |
| US20090246549A1 (en) | Glassy metal composite material | |
| CN102409194A (en) | Method for preparing foamed magnesium alloy special-shaped parts and composite parts by secondary foaming method | |
| Li et al. | Ultrafine-grained Ti66Nb13Cu8Ni6. 8Al6. 2 composites fabricated by spark plasma sintering and crystallization of amorphous phase | |
| US8414827B2 (en) | Porous light weight iron and method for preparing the same | |
| CN102676956B (en) | Method for preparing iron-based surface composite material by virtue of in-situ synthesis | |
| AU2014365267A1 (en) | Siliceous composition and method for obtaining same | |
| JP2002356754A (en) | Method for producing composite material and composite material produced by the method | |
| Ge et al. | Effect of CuO particle size on synthesis temperature and microstructure of Al2O3p–Al composites from Al–CuO system | |
| CN110699584B (en) | Preparation method of high-density low-strength low-plasticity alloy material for pulse impact energy absorption | |
| CN119506632B (en) | High specific gravity tungsten-refractory high entropy alloy composite material and preparation method thereof | |
| Griffo | Processing and physical metallurgy of tungsten-nickel aluminide composites | |
| CN105256260A (en) | Method for improving intensity of aluminum-based amorphous alloy |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08854041 Country of ref document: EP Kind code of ref document: A1 |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2010535889 Country of ref document: JP |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 12745121 Country of ref document: US |
|
| 32PN | Ep: public notification in the ep bulletin as address of the adressee cannot be established |
Free format text: NOTING OF LOSS OF RIGHTS PURSUANT TO RULE 112(1) EPC (EPO FORM 1205A DATED 09/08/2010) |
|
| 122 | Ep: pct application non-entry in european phase |
Ref document number: 08854041 Country of ref document: EP Kind code of ref document: A1 |